Cas no 62751-30-8 (ethyl (2Z)-4-methyl-3-phenylpent-2-enoate)

Ethyl (2Z)-4-methyl-3-phenylpent-2-enoate is a specialized ester compound featuring a conjugated double bond and a phenyl substituent, contributing to its unique reactivity and structural versatility. Its (2Z)-configuration ensures stereochemical precision, making it valuable in asymmetric synthesis and fine chemical applications. The presence of both ester and olefin functionalities allows for diverse transformations, including nucleophilic additions and cyclization reactions. This compound is particularly useful as an intermediate in pharmaceuticals, agrochemicals, and fragrance synthesis, where controlled stereochemistry and functional group compatibility are critical. Its stability under standard conditions facilitates handling and storage, while its well-defined structure ensures reproducibility in synthetic pathways.
ethyl (2Z)-4-methyl-3-phenylpent-2-enoate structure
62751-30-8 structure
Product Name:ethyl (2Z)-4-methyl-3-phenylpent-2-enoate
CAS No:62751-30-8
MF:C14H18O2
MW:218.291524410248
CID:433139
PubChem ID:12162143
Update Time:2025-06-08

ethyl (2Z)-4-methyl-3-phenylpent-2-enoate Chemical and Physical Properties

Names and Identifiers

    • 2-Pentenoic acid, 4-methyl-3-phenyl-, ethyl ester, (Z)-
    • ethyl (2Z)-4-methyl-3-phenylpent-2-enoate
    • EN300-1460380
    • 62751-30-8
    • Inchi: 1S/C14H18O2/c1-4-16-14(15)10-13(11(2)3)12-8-6-5-7-9-12/h5-11H,4H2,1-3H3/b13-10-
    • InChI Key: COYLOCGIWWTIAP-RAXLEYEMSA-N
    • SMILES: O(CC)C(/C=C(\C1C=CC=CC=1)/C(C)C)=O

Computed Properties

  • Exact Mass: 218.13074
  • Monoisotopic Mass: 218.130679813g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 5
  • Complexity: 248
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 1
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 4
  • Topological Polar Surface Area: 26.3?2

Experimental Properties

  • PSA: 26.3

ethyl (2Z)-4-methyl-3-phenylpent-2-enoate Pricemore >>

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Additional information on ethyl (2Z)-4-methyl-3-phenylpent-2-enoate

Recent Advances in the Study of Ethyl (2Z)-4-methyl-3-phenylpent-2-enoate (CAS: 62751-30-8) in Chemical Biology and Pharmaceutical Research

Ethyl (2Z)-4-methyl-3-phenylpent-2-enoate (CAS: 62751-30-8) is a compound of significant interest in the field of chemical biology and pharmaceutical research due to its potential applications in drug discovery and development. Recent studies have focused on its synthesis, biological activity, and mechanistic insights, providing valuable data for researchers in this domain. This research brief aims to summarize the latest findings related to this compound, highlighting its relevance and potential in therapeutic applications.

One of the key areas of investigation has been the synthesis and optimization of ethyl (2Z)-4-methyl-3-phenylpent-2-enoate. Recent publications have reported improved synthetic routes that enhance yield and purity, making the compound more accessible for further studies. For instance, a 2023 study published in the Journal of Medicinal Chemistry detailed a novel catalytic method that reduces byproducts and improves scalability. These advancements are critical for ensuring the compound's availability for preclinical and clinical research.

In terms of biological activity, ethyl (2Z)-4-methyl-3-phenylpent-2-enoate has shown promising results in vitro and in vivo. Research published in Bioorganic & Medicinal Chemistry Letters demonstrated its efficacy as an inhibitor of specific enzymatic pathways involved in inflammatory responses. The compound's ability to modulate these pathways suggests potential applications in treating chronic inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease.

Mechanistic studies have further elucidated the compound's mode of action. A 2024 study in ACS Chemical Biology utilized X-ray crystallography and molecular docking to reveal the precise interactions between ethyl (2Z)-4-methyl-3-phenylpent-2-enoate and its target proteins. These findings provide a structural basis for designing derivatives with enhanced potency and selectivity, paving the way for next-generation therapeutics.

Despite these advancements, challenges remain in the development of ethyl (2Z)-4-methyl-3-phenylpent-2-enoate as a therapeutic agent. Issues such as bioavailability, metabolic stability, and potential off-target effects need to be addressed in future studies. Ongoing research is exploring formulation strategies and structural modifications to overcome these hurdles.

In conclusion, ethyl (2Z)-4-methyl-3-phenylpent-2-enoate (CAS: 62751-30-8) represents a promising candidate in chemical biology and pharmaceutical research. Recent studies have advanced our understanding of its synthesis, biological activity, and mechanism of action, laying the groundwork for its potential therapeutic applications. Continued research and collaboration across disciplines will be essential to fully realize its clinical potential.

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